- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT05233969
Pain-Related Self-Efficacy in Individuals With Chronic Neck Pain
11. februar 2022 oppdatert av: MERVE KARAPINAR, Hacettepe University
An Investigation of Factors Affecting Pain-Related Self-Efficacy in Individuals With Chronic Neck Pain
The factors affecting pain-related self-efficacy in individuals with chronic neck pain were investigated.
A total of 69 subjects participated in the study.
After the demographic data of the subjects were taken, pain-self-efficacy questionnaire, Timed Up and Go Test, Berg Balance Scale and International Physical Activity Questionnaire were administered, respectively.
Studieoversikt
Status
Rekruttering
Forhold
Studietype
Observasjonsmessig
Registrering (Forventet)
69
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: MERVE KARAPINAR
- Telefonnummer: +905079089066
- E-post: mervekarapinar@gmail.com
Studiesteder
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-
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Isparta, Tyrkia
- Rekruttering
- Merve Karapinar
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Ta kontakt med:
- MERVE KARAPINAR
- Telefonnummer: +905079089066
- E-post: mervekarapinar1306@gmail.com
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-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
30 år til 65 år (Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Prøvetakingsmetode
Sannsynlighetsprøve
Studiepopulasjon
Adults with chronic neck pain
Beskrivelse
Inclusion Criteria;
- Adults aged 30 to 65 years,
- Adults with neck pain for at least 3 months,
- Having a score of 3 or more on the visual analog scale for pain ,
- To be willing to participate in the study.
Exclusion Criteria;
- Diagnosed with neurological, vestibular, rheumatic, or endocrine disorders,
- Had previous spinal surgery, neck trauma associated with post-traumatic amnesia or concurrent head injury, or cervical fracture or dislocation,
- currently receiving treatment for neck pathology.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Pain-Self-Efficacy Questionnaire(PSEQ)
Tidsramme: five minutes
|
The Pain Self-Efficacy Questionnaire is composed of 10 items assessing the patient's self-efficacy beliefs on performing a range of life activities taking pain into consideration.
Each item is rated on a 7-point Likert scale ranging from 0 = not at all confident to 6 = completely confident.
The maximum possible score is 60.
A high Pain Self-Efficacy Questionnaire score indicates a high level of belief in one's self-efficacy in performing life activities despite experiencing pain.
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five minutes
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Time Up and Go(TUG)
Tidsramme: five minutes
|
Patients were required to stand up from a chair with armrests, walk 3 meters, turn around, return to the chair and sit down as fast as possible.
The time taken to complete this task was recorded in seconds with a stopwatch.
Three trials were recorded per patient and the mean time to perform the task was calculated for each patient.
The mean time interval between each trial was 1 minute.
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five minutes
|
Berg Balance Scale(BBS)
Tidsramme: ten minutes
|
The BBS26 is a functional balance measurement and consists of 14 items.
Each item is a 5-point ordinal scale ranging from 0 to 4, with 0 indicating an inability to complete the task entirely and 4 indicating an ability to complete the task criterion.
Scores can range from 0 to 56.
The higher the score, the better the balance.
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ten minutes
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International Physical Activity Questionnaire(IPAQ)
Tidsramme: ten minutes
|
The IPAQ is used to assess habitual physical activitiy during the past 7 days.
The IPAQ used in the present study is the long version which covers four domains of physical activity: occupational (7 items), transportation (6 items), household/gardening (6 items) and leisure-time activities (6 items).
The questionnaire also includes two questions about the time spent on sitting as an indicator of sedentary behavior.
The number of days per week and the time spent on walking per day as well as moderate and vigorous activities from all four domains are recorded.
The IPAQ data were converted to metabolic equivalent scores (MET-min-week-1) for each type of activity, by multiplying the number of minutes dedicated to each activity class by the specific MET score for that activity.
Physical activity levels were also classified into three categories: inactive, minimally active and health-enhancing physically active, according to the scoring system provided by the IPAQ.
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ten minutes
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
1. februar 2022
Primær fullføring (Forventet)
20. mars 2022
Studiet fullført (Forventet)
30. juni 2022
Datoer for studieregistrering
Først innsendt
1. februar 2022
Først innsendt som oppfylte QC-kriteriene
1. februar 2022
Først lagt ut (Faktiske)
10. februar 2022
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
2. mars 2022
Siste oppdatering sendt inn som oppfylte QC-kriteriene
11. februar 2022
Sist bekreftet
1. februar 2022
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 326
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .
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